首页> 外文期刊>Dermatologic therapy >Efficacy and safety of basic fibroblast growth factor (bFGF) related decapeptide solution plus Tacrolimus 0.1% ointment versus Tacrolimus 0.1% ointment in the treatment of stable vitiligo
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Efficacy and safety of basic fibroblast growth factor (bFGF) related decapeptide solution plus Tacrolimus 0.1% ointment versus Tacrolimus 0.1% ointment in the treatment of stable vitiligo

机译:碱性成纤维细胞生长因子(BFGF)相关蒸馏菌溶液的功效和安全性Plus Tacrolimus 0.1%软膏与Tacrolimus 0.1%软膏治疗稳定的白癜风

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摘要

Abstract Vitiligo is common acquired pigmentary disorder affecting skin of 1% of the world population, India 3% to 8% incidences approximately. Treatment is tough challenge. The combination treatments have proven beneficial due to different mechanisms. There is need to find drug targeting different mechanisms of action. Test medicine is decapeptide derived from basic Fibroblast Growth Factor (bFGF) treating vitiligo. The current study was to compare efficacy and safety of BFGF related decapeptide solution plus Tacrolimus 0.1% (M?+?T) Ointment versus Tacrolimus monotherapy 0.1% (T) Ointment in patients with stable vitiligo. The randomized, open label, comparative, prospective, multicentre study in patients with stable vitiligo was conducted. The primary endpoint was improvement in extent of repigmentation in target lesion after 12?months of treatment from baseline. The secondary endpoints were extent of repigmentation at end of 6 months, patient global assessment (PGA) and safety at end of 6 months. This shows interim analysis results. Total 94 patients were randomized to M?+?T ( n = 40) and T ( n = 44), 10 patients were lost to follow up. Extent of repigmentation (50%) was significantly greater at end of 8?weeks in M?+?T group 22.5% ( p ?≤?.05) while 6.8% in T group. In grade of repigmentation, significant difference ( p ?≤?.05) was observed, M?+?T had better grade. PGA was significantly greater ( p ?≤?.05) in M?+?T‐group than T. All these parameters showed significant improvement in M?+?T‐group than group T at end of 6 months. No adverse events were reported during the study. It is an interim analysis report so complete data is not available for analysis. Addition of bFGF related decapeptide solution to Tacrolimus gave better results than Tacrolimus alone therapy. It also has a favorable safety profile and was well tolerated.
机译:摘要白癜风是常见的色素紊乱,影响了世界人口的1%,印度大约3%至8%。治疗是艰难的挑战。由于不同的机制,组合治疗已被证明是有益的。需要发现针对不同的行动机制。试验药是衍生自碱性成纤维细胞生长因子(BFGF)治疗白癜风的抑制肽。目前的研究是将BFGF相关的蒸馏孔溶液加上躯干蛋白氏菌溶液的功效和安全性与稳定的白癜风患者的软膏与Tacrolimus单疗法0.1%(t)软膏进行比较。进行了稳定的白癜风患者的随机,开放标签,比较,前瞻性,多期形研究。在从基线治疗的12个月治疗后,靶病变的重新沉降程度的改善程度是改善。次要终点在6个月结束时的重建程度,患者全球评估(PGA)和6个月末的安全性。这显示了临时分析结果。总共94名患者随机分配到m?+Δt(n = 40)和t(n = 44),10名患者失去跟进。在8℃的8个周末的成绩(& 50%)的程度明显更大?+Δt组22.5%(p?≤≤05),而T组6.8%。在重建等级中,观察到显着差异(P?≤≤05),M?+ΔT具有更好的等级。 PGA在m?+Δt组中显着更大(p≤≤≤05)。所有这些参数在6个月结束时显示M?+ΔT组的显着改善。在研究期间没有报告不良事件。它是一个中期分析报告,因此完整的数据不可用于分析。添加BFGF相关的Tacrolimus的Deapapidide溶液比单克莫司单独治疗产生了更好的结果。它还具有良好的安全性,并且具有良好的耐受性。

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